Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 11:36615033 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM961219 ; PhenCode RAG2base_HSRAG2X:g.1887G>A (C/T), RAG2base_RAG2_DNA:g.5754G>A (C/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 5156, 2010_April_001_278_RAG2_179616_0002

This variation has 7 HGVS names - click the plus to show

Variation displays